SRX956766 GSM1633892 SRP056164 SRS874402 GSM1633892 ChIP-Seq GENOMIC ChIP For ChIP of p300, sorted cells were incubated in fresh media with Flt3L for 2 hours before crosslinking; for ChIP of IRF8, Batf3, H3K27ac, and H3K4me1, cells fixed before purification. Cells were crosslinked with 1% formaldehyde, quenched with 1.25M Glycine, twice washed with PBS. Chromatin was sonicated for shearing DNA size from 140 to 500 bp. Chromatin fragments were immunoprecipitated overnight at 4 °C with Dynabeads Protein A or G bound to anti-p300 (sc-585X, Santa Cruz Biotechnology), anti-IRF-8 (sc-6058x, Santa Cruz Biotechnology), or anti-Batf3, anti-H3K27ac (Ab 4729, Abcam) and H3K4me1 (Ab 8895, Abcam). ChIPed DNA was eluted and reverse-crosslinked for 6 hr. DNA was purified with phenol:chloroform extraction followed by ethanol precipitation. Libraries for ChIP-seq were prepared using ThruPLEX-FD kit (Rubicon Genomics) and sequenced using Illumina HiSeq 2500 as single reads extending 50 bases. Illumina HiSeq 2500 GEO Sample GSM1633892 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1633892 gds 301633892 GEO Accession GSM1633892 SRX956767 GSM1633893 SRP056164 SRS874401 GSM1633893 ChIP-Seq GENOMIC ChIP For ChIP of p300, sorted cells were incubated in fresh media with Flt3L for 2 hours before crosslinking; for ChIP of IRF8, Batf3, H3K27ac, and H3K4me1, cells fixed before purification. Cells were crosslinked with 1% formaldehyde, quenched with 1.25M Glycine, twice washed with PBS. Chromatin was sonicated for shearing DNA size from 140 to 500 bp. Chromatin fragments were immunoprecipitated overnight at 4 °C with Dynabeads Protein A or G bound to anti-p300 (sc-585X, Santa Cruz Biotechnology), anti-IRF-8 (sc-6058x, Santa Cruz Biotechnology), or anti-Batf3, anti-H3K27ac (Ab 4729, Abcam) and H3K4me1 (Ab 8895, Abcam). ChIPed DNA was eluted and reverse-crosslinked for 6 hr. DNA was purified with phenol:chloroform extraction followed by ethanol precipitation. Libraries for ChIP-seq were prepared using ThruPLEX-FD kit (Rubicon Genomics) and sequenced using Illumina HiSeq 2500 as single reads extending 50 bases. Illumina HiSeq 2500 GEO Sample GSM1633893 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1633893 gds 301633893 GEO Accession GSM1633893 SRX956768 GSM1633894 SRP056164 SRS874400 GSM1633894 ChIP-Seq GENOMIC ChIP For ChIP of p300, sorted cells were incubated in fresh media with Flt3L for 2 hours before crosslinking; for ChIP of IRF8, Batf3, H3K27ac, and H3K4me1, cells fixed before purification. Cells were crosslinked with 1% formaldehyde, quenched with 1.25M Glycine, twice washed with PBS. Chromatin was sonicated for shearing DNA size from 140 to 500 bp. Chromatin fragments were immunoprecipitated overnight at 4 °C with Dynabeads Protein A or G bound to anti-p300 (sc-585X, Santa Cruz Biotechnology), anti-IRF-8 (sc-6058x, Santa Cruz Biotechnology), or anti-Batf3, anti-H3K27ac (Ab 4729, Abcam) and H3K4me1 (Ab 8895, Abcam). ChIPed DNA was eluted and reverse-crosslinked for 6 hr. DNA was purified with phenol:chloroform extraction followed by ethanol precipitation. Libraries for ChIP-seq were prepared using ThruPLEX-FD kit (Rubicon Genomics) and sequenced using Illumina HiSeq 2500 as single reads extending 50 bases. Illumina HiSeq 2500 GEO Sample GSM1633894 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1633894 gds 301633894 GEO Accession GSM1633894 SRX956769 GSM1633895 SRP056164 SRS874399 GSM1633895 ChIP-Seq GENOMIC ChIP For ChIP of p300, sorted cells were incubated in fresh media with Flt3L for 2 hours before crosslinking; for ChIP of IRF8, Batf3, H3K27ac, and H3K4me1, cells fixed before purification. Cells were crosslinked with 1% formaldehyde, quenched with 1.25M Glycine, twice washed with PBS. Chromatin was sonicated for shearing DNA size from 140 to 500 bp. Chromatin fragments were immunoprecipitated overnight at 4 °C with Dynabeads Protein A or G bound to anti-p300 (sc-585X, Santa Cruz Biotechnology), anti-IRF-8 (sc-6058x, Santa Cruz Biotechnology), or anti-Batf3, anti-H3K27ac (Ab 4729, Abcam) and H3K4me1 (Ab 8895, Abcam). ChIPed DNA was eluted and reverse-crosslinked for 6 hr. DNA was purified with phenol:chloroform extraction followed by ethanol precipitation. Libraries for ChIP-seq were prepared using ThruPLEX-FD kit (Rubicon Genomics) and sequenced using Illumina HiSeq 2500 as single reads extending 50 bases. Illumina HiSeq 2500 GEO Sample GSM1633895 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1633895 gds 301633895 GEO Accession GSM1633895 SRX956770 GSM1633896 SRP056164 SRS874398 GSM1633896 ChIP-Seq GENOMIC ChIP For ChIP of p300, sorted cells were incubated in fresh media with Flt3L for 2 hours before crosslinking; for ChIP of IRF8, Batf3, H3K27ac, and H3K4me1, cells fixed before purification. Cells were crosslinked with 1% formaldehyde, quenched with 1.25M Glycine, twice washed with PBS. Chromatin was sonicated for shearing DNA size from 140 to 500 bp. Chromatin fragments were immunoprecipitated overnight at 4 °C with Dynabeads Protein A or G bound to anti-p300 (sc-585X, Santa Cruz Biotechnology), anti-IRF-8 (sc-6058x, Santa Cruz Biotechnology), or anti-Batf3, anti-H3K27ac (Ab 4729, Abcam) and H3K4me1 (Ab 8895, Abcam). ChIPed DNA was eluted and reverse-crosslinked for 6 hr. DNA was purified with phenol:chloroform extraction followed by ethanol precipitation. Libraries for ChIP-seq were prepared using ThruPLEX-FD kit (Rubicon Genomics) and sequenced using Illumina HiSeq 2500 as single reads extending 50 bases. Illumina HiSeq 2500 GEO Sample GSM1633896 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1633896 gds 301633896 GEO Accession GSM1633896 SRX956771 GSM1633897 SRP056164 SRS874389 GSM1633897 ChIP-Seq GENOMIC ChIP For ChIP of p300, sorted cells were incubated in fresh media with Flt3L for 2 hours before crosslinking; for ChIP of IRF8, Batf3, H3K27ac, and H3K4me1, cells fixed before purification. Cells were crosslinked with 1% formaldehyde, quenched with 1.25M Glycine, twice washed with PBS. Chromatin was sonicated for shearing DNA size from 140 to 500 bp. Chromatin fragments were immunoprecipitated overnight at 4 °C with Dynabeads Protein A or G bound to anti-p300 (sc-585X, Santa Cruz Biotechnology), anti-IRF-8 (sc-6058x, Santa Cruz Biotechnology), or anti-Batf3, anti-H3K27ac (Ab 4729, Abcam) and H3K4me1 (Ab 8895, Abcam). ChIPed DNA was eluted and reverse-crosslinked for 6 hr. DNA was purified with phenol:chloroform extraction followed by ethanol precipitation. Libraries for ChIP-seq were prepared using ThruPLEX-FD kit (Rubicon Genomics) and sequenced using Illumina HiSeq 2500 as single reads extending 50 bases. Illumina HiSeq 2500 GEO Sample GSM1633897 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1633897 gds 301633897 GEO Accession GSM1633897 SRX956772 GSM1633898 SRP056164 SRS874397 GSM1633898 ChIP-Seq GENOMIC ChIP For ChIP of p300, sorted cells were incubated in fresh media with Flt3L for 2 hours before crosslinking; for ChIP of IRF8, Batf3, H3K27ac, and H3K4me1, cells fixed before purification. Cells were crosslinked with 1% formaldehyde, quenched with 1.25M Glycine, twice washed with PBS. Chromatin was sonicated for shearing DNA size from 140 to 500 bp. Chromatin fragments were immunoprecipitated overnight at 4 °C with Dynabeads Protein A or G bound to anti-p300 (sc-585X, Santa Cruz Biotechnology), anti-IRF-8 (sc-6058x, Santa Cruz Biotechnology), or anti-Batf3, anti-H3K27ac (Ab 4729, Abcam) and H3K4me1 (Ab 8895, Abcam). ChIPed DNA was eluted and reverse-crosslinked for 6 hr. DNA was purified with phenol:chloroform extraction followed by ethanol precipitation. Libraries for ChIP-seq were prepared using ThruPLEX-FD kit (Rubicon Genomics) and sequenced using Illumina HiSeq 2500 as single reads extending 50 bases. Illumina HiSeq 2500 GEO Sample GSM1633898 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1633898 gds 301633898 GEO Accession GSM1633898 SRX956773 GSM1633899 SRP056164 SRS874396 GSM1633899 ChIP-Seq GENOMIC ChIP For ChIP of p300, sorted cells were incubated in fresh media with Flt3L for 2 hours before crosslinking; for ChIP of IRF8, Batf3, H3K27ac, and H3K4me1, cells fixed before purification. Cells were crosslinked with 1% formaldehyde, quenched with 1.25M Glycine, twice washed with PBS. Chromatin was sonicated for shearing DNA size from 140 to 500 bp. Chromatin fragments were immunoprecipitated overnight at 4 °C with Dynabeads Protein A or G bound to anti-p300 (sc-585X, Santa Cruz Biotechnology), anti-IRF-8 (sc-6058x, Santa Cruz Biotechnology), or anti-Batf3, anti-H3K27ac (Ab 4729, Abcam) and H3K4me1 (Ab 8895, Abcam). ChIPed DNA was eluted and reverse-crosslinked for 6 hr. DNA was purified with phenol:chloroform extraction followed by ethanol precipitation. Libraries for ChIP-seq were prepared using ThruPLEX-FD kit (Rubicon Genomics) and sequenced using Illumina HiSeq 2500 as single reads extending 50 bases. Illumina HiSeq 2500 GEO Sample GSM1633899 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1633899 gds 301633899 GEO Accession GSM1633899 SRX956774 GSM1633900 SRP056164 SRS874395 GSM1633900 ChIP-Seq GENOMIC ChIP For ChIP of p300, sorted cells were incubated in fresh media with Flt3L for 2 hours before crosslinking; for ChIP of IRF8, Batf3, H3K27ac, and H3K4me1, cells fixed before purification. Cells were crosslinked with 1% formaldehyde, quenched with 1.25M Glycine, twice washed with PBS. Chromatin was sonicated for shearing DNA size from 140 to 500 bp. Chromatin fragments were immunoprecipitated overnight at 4 °C with Dynabeads Protein A or G bound to anti-p300 (sc-585X, Santa Cruz Biotechnology), anti-IRF-8 (sc-6058x, Santa Cruz Biotechnology), or anti-Batf3, anti-H3K27ac (Ab 4729, Abcam) and H3K4me1 (Ab 8895, Abcam). ChIPed DNA was eluted and reverse-crosslinked for 6 hr. DNA was purified with phenol:chloroform extraction followed by ethanol precipitation. Libraries for ChIP-seq were prepared using ThruPLEX-FD kit (Rubicon Genomics) and sequenced using Illumina HiSeq 2500 as single reads extending 50 bases. Illumina HiSeq 2500 GEO Sample GSM1633900 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1633900 gds 301633900 GEO Accession GSM1633900 SRX956775 GSM1633901 SRP056164 SRS874394 GSM1633901 ChIP-Seq GENOMIC ChIP For ChIP of p300, sorted cells were incubated in fresh media with Flt3L for 2 hours before crosslinking; for ChIP of IRF8, Batf3, H3K27ac, and H3K4me1, cells fixed before purification. Cells were crosslinked with 1% formaldehyde, quenched with 1.25M Glycine, twice washed with PBS. Chromatin was sonicated for shearing DNA size from 140 to 500 bp. Chromatin fragments were immunoprecipitated overnight at 4 °C with Dynabeads Protein A or G bound to anti-p300 (sc-585X, Santa Cruz Biotechnology), anti-IRF-8 (sc-6058x, Santa Cruz Biotechnology), or anti-Batf3, anti-H3K27ac (Ab 4729, Abcam) and H3K4me1 (Ab 8895, Abcam). ChIPed DNA was eluted and reverse-crosslinked for 6 hr. DNA was purified with phenol:chloroform extraction followed by ethanol precipitation. Libraries for ChIP-seq were prepared using ThruPLEX-FD kit (Rubicon Genomics) and sequenced using Illumina HiSeq 2500 as single reads extending 50 bases. Illumina HiSeq 2500 GEO Sample GSM1633901 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1633901 gds 301633901 GEO Accession GSM1633901 SRX956776 GSM1633902 SRP056164 SRS874393 GSM1633902 ChIP-Seq GENOMIC ChIP For ChIP of p300, sorted cells were incubated in fresh media with Flt3L for 2 hours before crosslinking; for ChIP of IRF8, Batf3, H3K27ac, and H3K4me1, cells fixed before purification. Cells were crosslinked with 1% formaldehyde, quenched with 1.25M Glycine, twice washed with PBS. Chromatin was sonicated for shearing DNA size from 140 to 500 bp. Chromatin fragments were immunoprecipitated overnight at 4 °C with Dynabeads Protein A or G bound to anti-p300 (sc-585X, Santa Cruz Biotechnology), anti-IRF-8 (sc-6058x, Santa Cruz Biotechnology), or anti-Batf3, anti-H3K27ac (Ab 4729, Abcam) and H3K4me1 (Ab 8895, Abcam). ChIPed DNA was eluted and reverse-crosslinked for 6 hr. DNA was purified with phenol:chloroform extraction followed by ethanol precipitation. Libraries for ChIP-seq were prepared using ThruPLEX-FD kit (Rubicon Genomics) and sequenced using Illumina HiSeq 2500 as single reads extending 50 bases. Illumina HiSeq 2500 GEO Sample GSM1633902 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1633902 gds 301633902 GEO Accession GSM1633902 SRX956777 GSM1633903 SRP056164 SRS874392 GSM1633903 ChIP-Seq GENOMIC ChIP For ChIP of p300, sorted cells were incubated in fresh media with Flt3L for 2 hours before crosslinking; for ChIP of IRF8, Batf3, H3K27ac, and H3K4me1, cells fixed before purification. Cells were crosslinked with 1% formaldehyde, quenched with 1.25M Glycine, twice washed with PBS. Chromatin was sonicated for shearing DNA size from 140 to 500 bp. Chromatin fragments were immunoprecipitated overnight at 4 °C with Dynabeads Protein A or G bound to anti-p300 (sc-585X, Santa Cruz Biotechnology), anti-IRF-8 (sc-6058x, Santa Cruz Biotechnology), or anti-Batf3, anti-H3K27ac (Ab 4729, Abcam) and H3K4me1 (Ab 8895, Abcam). ChIPed DNA was eluted and reverse-crosslinked for 6 hr. DNA was purified with phenol:chloroform extraction followed by ethanol precipitation. Libraries for ChIP-seq were prepared using ThruPLEX-FD kit (Rubicon Genomics) and sequenced using Illumina HiSeq 2500 as single reads extending 50 bases. Illumina HiSeq 2500 GEO Sample GSM1633903 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1633903 gds 301633903 GEO Accession GSM1633903 SRX956778 GSM1633904 SRP056164 SRS874391 GSM1633904 ChIP-Seq GENOMIC ChIP For ChIP of p300, sorted cells were incubated in fresh media with Flt3L for 2 hours before crosslinking; for ChIP of IRF8, Batf3, H3K27ac, and H3K4me1, cells fixed before purification. Cells were crosslinked with 1% formaldehyde, quenched with 1.25M Glycine, twice washed with PBS. Chromatin was sonicated for shearing DNA size from 140 to 500 bp. Chromatin fragments were immunoprecipitated overnight at 4 °C with Dynabeads Protein A or G bound to anti-p300 (sc-585X, Santa Cruz Biotechnology), anti-IRF-8 (sc-6058x, Santa Cruz Biotechnology), or anti-Batf3, anti-H3K27ac (Ab 4729, Abcam) and H3K4me1 (Ab 8895, Abcam). ChIPed DNA was eluted and reverse-crosslinked for 6 hr. DNA was purified with phenol:chloroform extraction followed by ethanol precipitation. Libraries for ChIP-seq were prepared using ThruPLEX-FD kit (Rubicon Genomics) and sequenced using Illumina HiSeq 2500 as single reads extending 50 bases. Illumina HiSeq 2500 GEO Sample GSM1633904 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1633904 gds 301633904 GEO Accession GSM1633904 SRX956779 GSM1633905 SRP056164 SRS874390 GSM1633905 ChIP-Seq GENOMIC ChIP For ChIP of p300, sorted cells were incubated in fresh media with Flt3L for 2 hours before crosslinking; for ChIP of IRF8, Batf3, H3K27ac, and H3K4me1, cells fixed before purification. Cells were crosslinked with 1% formaldehyde, quenched with 1.25M Glycine, twice washed with PBS. Chromatin was sonicated for shearing DNA size from 140 to 500 bp. Chromatin fragments were immunoprecipitated overnight at 4 °C with Dynabeads Protein A or G bound to anti-p300 (sc-585X, Santa Cruz Biotechnology), anti-IRF-8 (sc-6058x, Santa Cruz Biotechnology), or anti-Batf3, anti-H3K27ac (Ab 4729, Abcam) and H3K4me1 (Ab 8895, Abcam). ChIPed DNA was eluted and reverse-crosslinked for 6 hr. DNA was purified with phenol:chloroform extraction followed by ethanol precipitation. Libraries for ChIP-seq were prepared using ThruPLEX-FD kit (Rubicon Genomics) and sequenced using Illumina HiSeq 2500 as single reads extending 50 bases. Illumina HiSeq 2500 GEO Sample GSM1633905 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1633905 gds 301633905 GEO Accession GSM1633905